Canonical Allele Identifier: PA916039598
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411557
ClinVar RCV Id: RCV000565417 RCV002291636 RCV003651895 RCV004022879
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Leu566Val
CA16024895
NM_001354896.2:c.1696T>G